chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
103658695936586960A8GENIChomozygous132144862
103658849636588497AG13GENIChomozygous116561327
103659045336590454AG20GENIChomozygous116561331
103659066136590662GA12GENIChomozygous116561333
103659291436592915CG29GENIChomozygous116561335
103659360136593602AT18GENIChomozygous116561337
103659389836593899TC25GENIChomozygous116561339
103659446036594461CT13GENIChomozygous116868469
103659462436594625AC16GENICpossibly homozygous116868471
103659494336594944CT24GENIChomozygous116868473
103659584536595846GA18GENIChomozygous116868477
103659609936596100GA23GENIChomozygous116561341
103659636936596370GA16GENIChomozygous116868479
103659672236596723CT16GENIChomozygous116561343
103659676936596770T17GENIChomozygous128808040
103659680936596809GG16GENIChomozygous132144863
103659681036596811TG16GENIChomozygous132149675
103659687436596875AG13GENIChomozygous117409532
103660012936600130A20GENICpossibly homozygous128808043